Wuxi Beien Surgery Device Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Wuxi Beien Surgery Device Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wuxi, CN.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wuxi Beien Surgery Device Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mid-Link Consulting Co, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Wuxi Beien Surgery Device Co., Ltd.
1 devices